CHARACTERIZATION OF THE 3' END OF THE DELETION IN HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN (HPFH)

被引:0
|
作者
KAUFMAN, RE [1 ]
机构
[1] DUKE UNIV,MED CTR,DURHAM,NC 27710
来源
CLINICAL RESEARCH | 1982年 / 30卷 / 02期
关键词
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
引用
收藏
页码:A320 / A320
页数:1
相关论文
共 50 条
  • [31] HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN (HPFH) TOKUSHIMA VARIANT - UNEVEN DISTRIBUTION OF HBF AMONG RED-CELLS
    HASEGAWA, K
    KAWAI, H
    KANETO, Y
    NIKI, S
    YAMANO, T
    MIYOSHI, K
    JAPANESE JOURNAL OF HUMAN GENETICS, 1982, 27 (02): : 142 - 142
  • [32] HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN - REPLY
    MARTINEZ
    COLOMBO
    NATURE, 1975, 257 (5521) : 71 - 71
  • [33] HOMOZYGOSITY FOR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN
    KONOTEYAHULU, FID
    LANCET, 1979, 1 (8110): : 279 - 279
  • [34] Re-Creating Hereditary Persistence of Fetal Hemoglobin (HPFH) to Treat Sickle Cell Disease (SCD) and β-Thalassemia
    Lin, Michelle I.
    Paik, Elizabeth J.
    Mishra, Bibhu P.
    Chou, Song
    Zhang, Ying
    Tomkinson, Kaleigh
    Pettiglio, Michael A.
    Sanginario, Andrew
    Woo, Amanda
    Lee, Min Jin
    Allen, Melanie
    Cradick, Thomas J.
    Chakraborty, Tirtha
    Porteus, Matthew
    Lee, Ciaran M.
    Bao, Gang
    Miccio, Annarita
    Lattanzi, Annalisa
    Mavilio, Fulvio
    Cowan, Chad A.
    Novak, Rodger
    Lundberg, Ante S.
    BLOOD, 2016, 128 (22)
  • [35] Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype
    Hariharan, Priya
    Sawant, Madhavi
    Gorivale, Manju
    Manchanda, Ruma
    Colah, Roshan
    Ghosh, K.
    Nadkarni, Anita
    MOLECULAR BIOLOGY REPORTS, 2017, 44 (05) : 413 - 417
  • [36] Synergistic effect of two β globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype
    Priya Hariharan
    Madhavi Sawant
    Manju Gorivale
    Ruma Manchanda
    Roshan Colah
    K. Ghosh
    Anita Nadkarni
    Molecular Biology Reports, 2017, 44 : 413 - 417
  • [37] Flow cytometric measurement of hemoglobin F in RBCs - Diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-HPFH from other conditions with elevated levels of hemoglobin F
    Hoyer, JD
    Penz, CS
    Fairbanks, VF
    Hanson, CA
    Katzmann, JA
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2002, 117 (06) : 857 - 863
  • [38] THE MICROCHROMATOGRAPHIC ESTIMATION OF FETAL HEMOGLOBIN LEVELS IN HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN
    KRAUSS, JS
    JONAH, MH
    BAISDEN, CR
    PARNELL, DY
    NEELY, AE
    MOHORN, P
    CLINICAL CHEMISTRY, 1984, 30 (08) : 1419 - 1419
  • [39] Compound heterozygosity for the 532-bp deletion β thalassemia ano hereditary persistence of fetal hemoglobin (HPFH)-2 associated with thalassemia intermedia and extramedullary hematopoiesis.
    Qu, G
    Elkins, S
    Steinberg, MH
    JOURNAL OF INVESTIGATIVE MEDICINE, 2000, 48 (01) : 146A - 146A
  • [40] THE DELETION IN BOTH COMMON TYPES OF HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IS APPROXIMATELY 105 KILOBASES
    COLLINS, FS
    COLE, JL
    LOCKWOOD, WK
    IANNUZZI, MC
    BLOOD, 1987, 70 (06) : 1797 - 1803